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Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads : ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents. / Wang, Zhijia; Ivanov, Mikhail; Gao, Yuting и др.

в: Chemistry - A European Journal, Том 26, № 5, 22.01.2020, стр. 1091-1102.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Wang, Z, Ivanov, M, Gao, Y, Bussotti, L, Foggi, P, Zhang, H, Russo, N, Dick, B, Zhao, J, Di Donato, M, Mazzone, G, Luo, L & Fedin, M 2020, 'Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads: ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents', Chemistry - A European Journal, Том. 26, № 5, стр. 1091-1102. https://doi.org/10.1002/chem.201904306

APA

Wang, Z., Ivanov, M., Gao, Y., Bussotti, L., Foggi, P., Zhang, H., Russo, N., Dick, B., Zhao, J., Di Donato, M., Mazzone, G., Luo, L., & Fedin, M. (2020). Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads: ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents. Chemistry - A European Journal, 26(5), 1091-1102. https://doi.org/10.1002/chem.201904306

Vancouver

Wang Z, Ivanov M, Gao Y, Bussotti L, Foggi P, Zhang H и др. Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads: ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents. Chemistry - A European Journal. 2020 янв. 22;26(5):1091-1102. doi: 10.1002/chem.201904306

Author

BibTeX

@article{44515af85b3e4a0e80ebb3a409330ced,
title = "Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads: ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents",
abstract = "Spin–orbit charge-transfer intersystem crossing (SOCT-ISC) is useful for the preparation of heavy atom-free triplet photosensitisers (PSs). Herein, a series of perylene-Bodipy compact electron donor/acceptor dyads showing efficient SOCT-ISC is prepared. The photophysical properties of the dyads were studied with steady-state and time-resolved spectroscopies. Efficient triplet state formation (quantum yield ΦT=60 %) was observed, with a triplet state lifetime (τT=436 μs) much longer than that accessed with the conventional heavy atom effect (τT=62 μs). The SOCT-ISC mechanism was unambiguously confirmed by direct excitation of the charge transfer (CT) absorption band by using nanosecond transient absorption spectroscopy and time-resolved electron paramagnetic resonance (TREPR) spectroscopy. The factors affecting the SOCT-ISC efficiency include the geometry, the potential energy surface of the torsion, the spin density for the atoms of the linker, solvent polarity, and the energy matching of the 1CT/3LE states. Remarkably, these heavy atom-free triplet PSs were demonstrated as a new type of efficient photodynamic therapy (PDT) reagents (phototoxicity, EC50=75 nm), with a negligible dark toxicity (EC50=78.1 μm) compared with the conventional heavy atom PSs (dark toxicity, EC50=6.0 μm, light toxicity, EC50=4.0 nm). This study provides in-depth understanding of the SOCT-ISC, unveils the design principles of triplet PSs based on SOCT-ISC, and underlines their application as a new generation of potent PDT reagents.",
keywords = "Bodipy, electron spin polarization, perylenes, photodynamic therapy, spin–orbital charge-transfer intersystem crossing (SOCT-ISC), RECOMBINATION, EXCITED-STATE, UP-CONVERSION, TIME-RESOLVED EPR, PHOTOSENSITIZERS, PARAMAGNETIC-RESONANCE, TRIPLET-STATE FORMATION, spin-orbital charge-transfer intersystem crossing (SOCT-ISC), SINGLET OXYGEN GENERATION, RADICAL-ION PAIRS, BODIPY DERIVATIVES",
author = "Zhijia Wang and Mikhail Ivanov and Yuting Gao and Laura Bussotti and Paolo Foggi and Huimin Zhang and Nino Russo and Bernhard Dick and Jianzhang Zhao and {Di Donato}, Mariangela and Gloria Mazzone and Liang Luo and Matvey Fedin",
note = "{\textcopyright} 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.",
year = "2020",
month = jan,
day = "22",
doi = "10.1002/chem.201904306",
language = "English",
volume = "26",
pages = "1091--1102",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-VCH Verlag",
number = "5",

}

RIS

TY - JOUR

T1 - Spin–Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor–Acceptor Dyads

T2 - ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents

AU - Wang, Zhijia

AU - Ivanov, Mikhail

AU - Gao, Yuting

AU - Bussotti, Laura

AU - Foggi, Paolo

AU - Zhang, Huimin

AU - Russo, Nino

AU - Dick, Bernhard

AU - Zhao, Jianzhang

AU - Di Donato, Mariangela

AU - Mazzone, Gloria

AU - Luo, Liang

AU - Fedin, Matvey

N1 - © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

PY - 2020/1/22

Y1 - 2020/1/22

N2 - Spin–orbit charge-transfer intersystem crossing (SOCT-ISC) is useful for the preparation of heavy atom-free triplet photosensitisers (PSs). Herein, a series of perylene-Bodipy compact electron donor/acceptor dyads showing efficient SOCT-ISC is prepared. The photophysical properties of the dyads were studied with steady-state and time-resolved spectroscopies. Efficient triplet state formation (quantum yield ΦT=60 %) was observed, with a triplet state lifetime (τT=436 μs) much longer than that accessed with the conventional heavy atom effect (τT=62 μs). The SOCT-ISC mechanism was unambiguously confirmed by direct excitation of the charge transfer (CT) absorption band by using nanosecond transient absorption spectroscopy and time-resolved electron paramagnetic resonance (TREPR) spectroscopy. The factors affecting the SOCT-ISC efficiency include the geometry, the potential energy surface of the torsion, the spin density for the atoms of the linker, solvent polarity, and the energy matching of the 1CT/3LE states. Remarkably, these heavy atom-free triplet PSs were demonstrated as a new type of efficient photodynamic therapy (PDT) reagents (phototoxicity, EC50=75 nm), with a negligible dark toxicity (EC50=78.1 μm) compared with the conventional heavy atom PSs (dark toxicity, EC50=6.0 μm, light toxicity, EC50=4.0 nm). This study provides in-depth understanding of the SOCT-ISC, unveils the design principles of triplet PSs based on SOCT-ISC, and underlines their application as a new generation of potent PDT reagents.

AB - Spin–orbit charge-transfer intersystem crossing (SOCT-ISC) is useful for the preparation of heavy atom-free triplet photosensitisers (PSs). Herein, a series of perylene-Bodipy compact electron donor/acceptor dyads showing efficient SOCT-ISC is prepared. The photophysical properties of the dyads were studied with steady-state and time-resolved spectroscopies. Efficient triplet state formation (quantum yield ΦT=60 %) was observed, with a triplet state lifetime (τT=436 μs) much longer than that accessed with the conventional heavy atom effect (τT=62 μs). The SOCT-ISC mechanism was unambiguously confirmed by direct excitation of the charge transfer (CT) absorption band by using nanosecond transient absorption spectroscopy and time-resolved electron paramagnetic resonance (TREPR) spectroscopy. The factors affecting the SOCT-ISC efficiency include the geometry, the potential energy surface of the torsion, the spin density for the atoms of the linker, solvent polarity, and the energy matching of the 1CT/3LE states. Remarkably, these heavy atom-free triplet PSs were demonstrated as a new type of efficient photodynamic therapy (PDT) reagents (phototoxicity, EC50=75 nm), with a negligible dark toxicity (EC50=78.1 μm) compared with the conventional heavy atom PSs (dark toxicity, EC50=6.0 μm, light toxicity, EC50=4.0 nm). This study provides in-depth understanding of the SOCT-ISC, unveils the design principles of triplet PSs based on SOCT-ISC, and underlines their application as a new generation of potent PDT reagents.

KW - Bodipy

KW - electron spin polarization

KW - perylenes

KW - photodynamic therapy

KW - spin–orbital charge-transfer intersystem crossing (SOCT-ISC)

KW - RECOMBINATION

KW - EXCITED-STATE

KW - UP-CONVERSION

KW - TIME-RESOLVED EPR

KW - PHOTOSENSITIZERS

KW - PARAMAGNETIC-RESONANCE

KW - TRIPLET-STATE FORMATION

KW - spin-orbital charge-transfer intersystem crossing (SOCT-ISC)

KW - SINGLET OXYGEN GENERATION

KW - RADICAL-ION PAIRS

KW - BODIPY DERIVATIVES

UR - http://www.scopus.com/inward/record.url?scp=85077975932&partnerID=8YFLogxK

U2 - 10.1002/chem.201904306

DO - 10.1002/chem.201904306

M3 - Article

C2 - 31743947

AN - SCOPUS:85077975932

VL - 26

SP - 1091

EP - 1102

JO - Chemistry - A European Journal

JF - Chemistry - A European Journal

SN - 0947-6539

IS - 5

ER -

ID: 23209884